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By J. Ipinza

The slime formation with several metallic impurities from acidic electrolytes of copper has been studied. On fresh Pb-Ca-Sn anode surface firstly the formation of PbSO4 takes place, then, it is transformed in the conducting PbO2, which covers the anode surface. It has been experimentally established the formation of a manganese dioxide double layer at the anode; this double layer was always composed of a thick external layer of non-adhering and easily removable scales, and of a thin internal layer, which adheres relatively well to the surface of the electrode. It was found that manganese dioxides present in the slime were of different nature: a non-adhering layer produced by electrolysis (-MnO2) on the PbO2 surface and a pure chemical precipitation in the solution (-MnO2). When iron is present in the electrolyte on this last layer of manganese, lead sulfate was found. In the case of arsenic and antimony in the electrolyte the slime generated was found to be lead sulfate and amorphous compounds of those ions. The lower slime generation in Chilean EW plants could be due to the lower contents of iron and manganese in the electrolytes. It was found that this slime formation rate not only is due to the electrolyte composition but also to the poor control of operational parameters at EW plants.

Jan 1, 2003

By Jin-Chun Kim

Nanosized W based powders (W, WC, WC-Co) were produced by chemical vapor condensation (CVC) process. Two different solid W(CO)6 and Co2(CO)8 metal-organic materials were used as precursors. CVC experiment was conducted in the temperature range of 400-1100. As-CVC WC1-x powder which had non-stoichiometric composition was carburized by using of the CH4-H2 mixed gas in temperature range of 750-850. The CVC W and WC1-x powders showed loosely agglomeration structure, and the Co powder had intricate long stand structure because of intrinsic magnetic properties of Co phase. Carbon content of the CVC powders controlled by gas-phase carburization was well matched with theoretical WC stoichiometry (6.13wt%).

Jan 1, 2006

By Bernard Bonnetot

The potentialities of hydrogen storage using borohydrides are presented and discussed especially in regard to the recoverable hydrogen amount and to the recovery conditions. A rapid analysis of storage possibilities is proposed taking in account the two main ways for hydrogen evolution: the dehydrogenation obtained using thermal decomposition of borohydrides or the hydrolysis of solid or dissolved borohydrides. The recoverable hydrogen is related to the dehydrogenation conditions and the real hydrogen useful percentage is determined for each case of use. The high temperatures required for dehydrogenation, even using catalyzed borohydrides, lead to poor outlooks for this storage technique. The hydrolysis conditions fix the yield of the recovered hydrogen and rule the storage capacity of the dissolved borohydride, the "fuel".

Jan 1, 2006

By M. Urda-Kiel

Stainless steel is increasingly used as a cathode starting sheet. It was shown earlier that even when depositing copper on copper, a substrate-influenced zone appears in the deposit structure, followed by a transition zone and finally by the electrolysis-influenced structure. On copper, the substrate-influenced zone has a thickness of twenty micrometers and on titanium, eventually more than fifty micrometers. Initial nucleation and growth have a considerable influence. In this paper, copper was deposited in a channel cell on four different 304 stainless steel substrates: mechanically polished and anodized, respectively, at 0, +400 and +800 mV/SHE in 1M H2SO4 at 20°C. Copper was deposited under electrowinning conditions after solvent extraction (SX) (40 g/l Cu++, 180 gh/l, H2SO4, 20 or 60°C). The results showed that, although Auger surface analyses of the substrates were only slightly different one from another including the oxide thickness, nucleation and initial stages of growth were very sensitive to the surface treatment of the substrate. Potential step and current step methods gave similar results : progressive nucleation followed by 3D diffusion controlled growth. The highest nucleation frequency was observed on stainless steel anodized at 0 mV/SHE, under various electrolysis conditions. The potential influence of these findings on industrial practice is discussed.

Jan 1, 1999

By Weng Fu

In this study, Resin-in-Pulp (RIP) technology is used to separate Pb from a chalcopyrite slurry. Solvent-impregnated resin, Lewatit® VP OC 1026, which contains di(2-ethylhexyl) phosphoric acid (D2EHPA) in a macroporous polystyrene matrix was used, as the functional group exhibits selectivity for Pb over Cu. Adsorption pH, kinetics, as well as resin and CuSO4 concentrations were investigated. The results show that the kinetics of Pb and Cu loading are fast, reaching the adsorption equilibrium within 30 min. The equilibrium pH of 2 was chosen as optimum for operation in order to achieve a high Pb extraction rate and extent as well as selectivity for Pb over Cu. High Cu(II) concentration in solution results in Pb(II) requiring a larger amount of resin for the same degree of extraction. Regeneration and reuse tests show that the loss of adsorption capacity happens in the 1st and 2nd cycles and then the adsorption capacity stabilises for the 3rd cycle.

By Pieter Steeneklm, Mazi’ Rejaee

"EXECUTIVE SUMMARYThe automotive industry's search for increased fuel efficiency through component weight reduction has driven the growth in consumption of magnesium metal in the form of die cast alloys. This trend, which began in North America and should soon accelerate in Europe, will require enhanced recycling services since each tonne of metal used for die cast parts production produces about 500 kg of scrap.Currently, the European die cast market is plagued by very high tolling prices for scrap recycling due to lack of competition and high transport costs due to the distances between the scrap generator and the recycling facility. This situation clearly increases the cost of magnesium die cast components and reduces magnesium's competitiveness with other materials. The challenge for the magnesium industry in the short term is to provide cost ·effective recycling solutions for the die cast industry. In addition effective recycling, in the medium to long term, is needed for the anticipated large volumes of secondary or used scrap that will become available as the die cast components reach the end of their life cycle. This paper will present The Antheus Integrated Magnesium Project as a Novel approach addressing some of the key recycling related issues facing the magnesium industry, in particular the die casters. The paper outlines the many advantages of an integrated magnesium metal park, in an overall goal of increasing magnesium metal's competitiveness."

Jan 1, 2000

By Robert F. Jenkins, King G. Robertson

This paper presents a practical approach for utilizing a computer model to determine the mass balance for a typical UBC recycling complex - starting with raw materials input, through scrap preparation, delacquering, melting, alloy adjustment and casting. This model is especially concerned with metal unit losses throughout the recycling complex with emphasis on metal losses at the melting furnace. The model also addresses the application of hardener alloys, metallurgical salts, chlorine for demagging, and reagents for acid gas emissions control. Other issues addressed are dross generation, acid gas emissions and dirt and fines to landfill. One benefit of the model is the conversion of annual production objectives to hourly production rates and resource requirements taking into account production schedules, maintenance downtime, and operations inefficiencies.

Jan 1, 2000

By W. B. Carter, A. T. Hunt, G. W. Book

"Combustion Chemical Vapor Deposition (CCVDSM ), an open air, flame assisted CVD process, is under development. The CCVD process produces non-line-of-sight, epitaxial deposition. Materials deposited include YBa2Cu3Ox' Y2BaCuOx, BaTiO3, Y2FesOI2, ZrO2, yttria stabilized ZrO2 (YSZ), partially (yttria) stabilized ZrO2 (PSZ), and amorphous silica. Two modifications of the CCVD process are being studied. Liquid fuel CCVD deposition, involves the combustion of an organic solvent that contains dissolved reagents carrying the desired coating cations. Gaseous fuel CCVD deposition uses a flammable gas as fuel. A non-flammable solution containing dissolved reagents is either aspirated into the flame or mixed with the fuel gas as an aerosol prior to its combustion. Substrates to be coated are held near the flames' ends.IntroductionThin films and coatings can be deposited using a wide variety of techniques including chemical vapor deposition (CVD). CVD is ""a materials synthesis process whereby constituents of the vapor phase react chemically near or on a substrate surface to form a solid product.""lIn conventional CVD processing, gases carrying coating constituents flow into a reaction vessel where deposition occurs onto a heated substrate. The deposition process is often conducted at reduced pressure. Both cold and hot wall reaction chambers are used. Heat can be provided by a resistance furnace, rf induction, or high-intensity radiation lamps. Plasma, microwave, photo, laser, RF, and electron-enhanced CVD processes have been developed. The necessity of using a reaction vessel limits the substrate size and affects coating economics. Although most CVD depositions are performed as batch processes, continuous deposition can be accomplished with the use of appropriate hardware.The chemical vapor deposition of thin, dense oxide films has been accomplished in the open atmosphere with a flame assisted process. The process is called combustion chemical vapor deposition (CCVDSM).2 Two modifications of the CCVD process have been developed. The liquid fuel CCVD process involves the combustion of an organic solvent in which reagents (containing the coating cations) are dissolved. The gaseous fuel CCVD process uses a flammable gas as fuel. In this modification, a non-flammable solution containing dissolved reagents is either aspirated into the flame or mixed with the fuel gas as an aerosol of small droplets prior to its combustion. Substrates to be coated are held near the flames' ends."

Jan 1, 1994

By I. Hilario, D.Y. Medina, V.J. Cortés, J.D. Muñoz

The process of Tribofinishing is investigated as a memns to reacha state of quality for the surface teated. During the said process there occurs mass transferat the interface of the piece to be treated and the abrasive charge (abrasive plus additives). This stiuation is studied for Titanium as a possibility for application in prosthesis. With these results is intended to produce a model of the mass transfer that would allow having further control of the process.

Jan 1, 2012

By Wenying Liu

The effect of aeration on chalcocite heap leaching was studied by analyzing the historical data from two chalcocite heap leach pads located in Chile, one with aeration and the other without aeration. The data showed that the copper leaching kinetics of the aerated heap was greater than that of the unaerated heap within a certain leaching period, after which there was no effect of aeration on the copper leaching kinetics. The total acid consumption per ton of ore processed was higher in the case of aeration, which was supported by the higher pH of the PLS. But the net acid consumption per ton of copper produced was the same in the two cases. Approximately 5% of the total iron added to the unaerated heap was precipitated inside the heap. In contrast, there was no net iron precipitation or generation inside the aerated heap. Bacteria activities were thought to occur even in the unaerated heap, but the extent was much less than in the aerated heap. Given the importance of forced aeration in chalcocite heap bioleaching, mathematical modelling will be applied in the future work to assist the optimization of the aeration system design.

By S. Kawamura, H. Inoue, Y. Maeda, H. Ohike

Kosaka smelter is a copper smelter located in Akita Prefecture in the northern part of Japan. It has treated complex sulfide concentrates for a long time. Recently, in addition to metal production from ores, the company has been working on the recycling of metals by using this metallurgical technology. Metals recovered are primarily gold, silver, palladium, copper and lead from copper scraps, electronic board scraps, silver oxide batteries, spent lead acid batteries, semiconductor chips, cellular phones, and automotive emissions catalyst. In particular, electronic board scraps and cellular phones can be valuable raw materials. These electronic scraps are fed into the flash smelting furnace after size reduction in a shredder that was introduced in 1999. Due to the growing demand for personal computers and cellular phones, the amount of electronic board scraps available for recycling increased. At present, these secondary materials are good raw materials for Kosaka smelter since the smelter is already used to dealing with complex raw materials. The recycled metals account for up between 5 and 20 percent of the total production at Kosaka Smelter. In particular, over 90 percent of the palladium in the secondary materials can be recovered.

Jan 1, 2000

By R. D. Prengaman

Lead usage in paint, anti-knock gasoline additives, pipes, seals, and solder has declined markedly over the past 30 years. Products utilizing the unique properties of lead and its ability to be recycled have survived and grown. These products include shielding, glass (particularly TV and computer screens), sheet for roofing, stabilizers for PVC, insoluble anodes for metal production, electronic solders and lead acid batteries. With the loss of markets many companies have decreased lead product development efforts. Much of the patent lead materials development is devoted to lead acid batteries. In the past 25 years, the automobile battery has been almost doubled in power and reduced in weight, leading to a nearly three-fold increase in performance. Corrosion-resistant lead alloys and improved battery designs have made battery lead usage more efficient. The same corrosion-resistant battery alloys are utilized to increase the life of electrowinning anodes. The challenge for lead product development is not only to maintain and improve the existing lead products, but also to develop the growing lead acid battery market for telecommunications, uninterruptive power sources, remote area power, hybrid and electric vehicles. Lead

Jan 1, 2000

By Hiroshi Maeta, Takao Kino, Hirota Osono, Kikuo Matsusaka, Azusa Shida

"Prior to refine an ultra-high purity material, it is necessary to estimate the surface cleanness of a base material. In this report, the cleaning method of a surface for refining of an ultra-high purity aluminum has been studied. Aluminum sample of 99.999% purity was p9lished mechanically and electrically and washed with various solvents. Surface composition and a depth profile near the surface were examined. Based on the experimental results, surface structure of an ultra-high purity aluminum was discussed.IntroductionRecently, studies on high purity metals have become of interest, and we have reported .various properties of an ultra- high purity aluminum1- 2)In order to purify a metal, it is necessary to clean a work area and to make vacuous as possible. So, we are studying the purification of aluminum by an ultra-high vacuum refining system and a zone refining system set up in a clean room with cleanliness class of 1000.Now, in order to avoid a mixing of impurities into the refining metal, a surface cleanness of a base metal is very important factor. The purity of the base aluminum used our work is 99.999%, but the surface state of the base aluminum is not clear. Aims in this work .are to investigate the surface state and to obtain the cleaning method of the base aluminum.Experimental procedureSamples used in this work were 99.9% (3N), 99.99%(4N) and 99.999% (SN) aluminum produced industrially and 99.9999% (6N) aluminum purified by us."

Jan 1, 2000

By G. Gerbeth, Y. Gelfgat, A. Cramer, A. Bojarevics

The production of highly porous metallic substrates requires an effective and well controlled production of metallic fibres with diameters in the range of 50 to 200 microns. The melt extraction, where a quickly rotating wheel extracts fibres directly out of the inductively heated melt, is a promising technology for that purpose. The main limitations of this process are due to turbulence within the melt and a wavy motion on the surface. Both effects give rise to strong and time dependent deformation of the melt surface which, in turn, causes non-stationary conditions of the contact zone between the extraction wheel and the melt. In the patent literature many examples can be found which try to overcome these problems by submersing mechanical parts directly into, or placing them at least in close vicinity to the melt, aiming at a stabilisation of that contact region. Even made of heat resistant ceramics they suffer from corrosion or cracks and do not work reliable at all. The present work describes a non invasive control mechanism by means of a magnetic field. Model experiments were carried out to study the calm down of the turbulent surface of a inductively stirred melt. The stabilisation of the melt surface has been demonstrated in practise by the installation of a solenoid at a working extraction facility under rough industrial conditions like a powerful induction heating and vacuum.

Jan 1, 1999

By K. Morsi, P. Mehra

"Spark plasma sintering has gained a considerable amount of attention over the past decade, due to its rapid sintering rates, and low temperature requirements, but has so far been usually limited to the production of simple geometries. The present paper examines the current-activated production of extended geometries through the process of spark plasma ""extrusion"". Of interest in the present study is exploratory research into the effect of electrical current activation on the reactive consolidation of powder systems to form intermetallic materials.IntroductionSpark Plasma Sintering (SPS) has been the subject of intense research over the past decade [ 1,2, 3,4,5,6]. The process boasts unique advantages which include ultra fast heating rates, shorter sintering times and lower sintering temperatures than needed in conventional sintering. The process is however limited to the generation of predominantly simple geometries. Recently one of the authors investigated the spark plasma extrusion of aluminum, where an aluminum powder compact is directly (Joule) heated through an applied DC electric current. Here extended geometries can be generated under the influence of electric current. A number of heating sources were identified including the heat source from current, i.e. Joule heating, frictional heating and heat from the deformation energy. However in the case of reactive powder systems, an extra ""one-time"" transient heating source can be supplied. By considering combustion synthesis of powders, this heating source is derived from the reaction between elemental powders to exothermically form a product at some ignition temperature [7]. This exothermic energy heats the compact to the maximum ""combustion temperature'', which could be hundreds of degrees higher than the ignition temperature. Hence a high temperature processing window (of short duration due to heat losses to the surroundings) becomes available in which the material is most suitable for stress-induced deformation and consolidation. For reactive spark plasma extrusion, two scenarios can be envisioned. The first is where the reactive powder compact is ignited through the application of current, and extruded within the high temperature processing window (also under the influence of current). The second scenario is to allow the heat of deformation/friction to heat the material during extrusion, to simultaneously force a reaction and consolidation. Here it is expected that the processing window will be very small if feasible."

Jan 1, 2011

By Eduardo Juncal, Jorge Alberto Soares Tenorio, Jose Roberto de Oliveira, Denise Crocce Romano Espinosal

"Steel industry has been expanding every year, consequently there has been an increase in waste generation in this area. Thus, companies in this sector are finding it difficult to give a correct destination of waste. For example, only in a basic oxygen furnace (BOF) converter are generated about l8kg of dust per ton of steel. The aim of this work was the characterization of dust generated in the BOF converter. The characterization was performed by chemical analysis (titration for iron and its oxides and Inductively Coupled Plasma Atomic Emission Spectroscopy for other elements), scanning electron microscopy, size analysis using Mastersizer 2000 equipment and X-ray diffraction. It was observed that dust is composed mainly iron in form of magnetite, metallic iron and wustite with approximately 99% of the particle size below 100 µm.IntroductionToday, steel is a important metal for the world. It can be produced for two routes, blast furnace/ basic oxygen furnace (BOF) converter and electric arc furnace (EAF) [1].First route, the iron is produced from the reduction of iron ore and coke for fuel injection and! or natural gas for a production of pig iron in blast furnace. The pig iron is sent until BOF converter to perform the blowing of oxygen to obtain the steel. In the second route, the steel is produced using scraps or direct reduced iron (DR!) using electric arc.During steel production are generated a lot of wastes like slag, sludges, scraps and dust [2]. Only in the first six months of201O, world steel production totaled 706 million tons [3]. According to Watson and Wang [4], some 10 to 20 kg of dust is generated per tonne of liquid steel produced. Thus, the reuse of these wastes can be a great to companies, because it reduces the amount of raw material to be extracted and reducing disposal costs [5,6]."

Jan 1, 2012

By Reuben John Mathew

"Oxygen evolution is the main anode reaction in industrial copper electrowinning. The oxygen bubbles do not conduct electricity, thus increasing the electrolyte resistance. The oxygen bubbles formed at the anode rise to the surface, occupying a larger volume of the electrolyte at the top of the cell than at the bottom. This oxygen bubble concentration gradient contributes to a gradient in electrolyte resistance and consequently a tendency toward uneven current distribution. This phenomenon increases the chance for uneven growth on the cathode and/or short-circuits, particularly on the lower portions of the cathode. This issue may be ameliorated by increasing the charge transfer resistance for oxygen evolution down the height of the anode. This concept was studied by solving the current distribution for a 2-D model of a copper electrowinning cell using COMSOL.IntroductionA copper electrowinning tankhouse aims to operate at the highest current density that will deposit on the cathode a layer of copper metal possessing the desired physical and chemical characteristics. The operating current density is directly related to the physical nature of the copper deposit on the cathode (Figure 1), limiting a copper electrowinning tankhouse to some operating current density that produces acceptable copper deposits.[!] The ratio of the operating current density to the limiting current density is typically around 0.3.[2] If the limiting current density for a cell could be raised, the operating current density could also be raised and thus result in savings in capital cost for a tankhouse. [3]The average operating current density in a copper electrowinning plant is 270A·m- 2 .[4] The value for average current density, however, obscures the fact that the face of a cathode does not experience this value equally. Indeed, the current density varies along the height of an electrode and is independent of the height of the electrode.[5] This phenomenon partly explains why the lower portions of a cathode tend to display a rougher copper deposit.In order to utilize a higher operating current density but still remain at 30% of the limiting current density, the limiting current density must be raised, but it is affected by the mass transfer regime at the electrodes. The mass transfer regime is currently poorest at the lower portions of the cathode and this is part of the reason for the tendency for poor cathode deposits to occur at the lower portion of the cathode.[6]"

Jan 1, 2012

By T. Goda, H. Kiuchi, M. Iguchi

"IntroductionThe utilization of silver in the electronic industry has been increasing in recent years. It is desirable that valuable metals are recovered from the used scraps of these industrial goods. Condensor chips, for example, contain silver, palladium, and Ag-Pd alloy. The dissolution behavior of silver was studied assuming that scraps such as used condensor chips in which Ag-Pd paste is used are subjected to wet treatment.ExperimentalIn this study the powder, granules, and flakes of silver were used in these nitric acid leaching experiments. The nitric acid solution was agitated in a glass reactor with a magnetic stirrer and heated to the required temperature. The experiment was started by putting the silver sample in the solution. After the leaching, the solution was filtered and the concentration of silver in the filtrate was analyzed by ICP.ResultsIn dilute nitric acid of less than 5 N, silver powder dissolved easily with increase in the concentration of nitric acid and temperature. However, the more intensive the stirring of the solution was, the lower the dissolution quantity became. Fig. 1"

Jan 1, 2000

By Ian M. Ritchie

Right across the universities of the developed world, the traditional disciplines of physics and chemistry are losing ground. Extractive metallurgy, which depends so heavily on chemistry, is also contracting despite a clear need for people with this kind of training in the mining industry. Reasons for this loss of popularity are discussed in this paper. High on the list is one of image. The extraction of metals is widely seen as a dirty, polluting, sunset industry which involves working in remote and uncomfortable corners of the earth for inadequate compensation. Ways in which the image problem can be overcome are considered. It is concluded that a concerted effort needs to be made by the universities and industry to redress this situation. The importance of extractive metallurgy, both now and in the future, when a greater emphasis will be placed on sustainability and recycling, needs to be stressed. In addition, courses need to incorporate training for a career path that leads on beyond extractive metallurgy.

Jan 1, 2003

By M. Misra

The volume of low-level contaminated soil at the. Department of Energy's Nuclear Weapon Sites are in the order of several million tons. Most of the contaminants are uranium, plutonium, other heavy metals and organic compounds. Selected Physical separation processes have shown demonstrated potential in COD Centratingthe radio nuclides in a small fraction of the soil. Depending upon the size, nature of bonding and distributions of radio nuclides, more than 90 percent of the radio nuclide activity can be concentrated in a small volume of fraction of the soil. The physico-chemical separation processes such as flotation in a mechanical and microbubble tall column cell have shown, promising applications in cleaning up the high volume contaminated soil.

Jan 1, 1995